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1.
Int J Colorectal Dis ; 31(11): 1759-1766, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27614446

RESUMEN

PURPOSES: The objective of this study was to evaluate the effect of supplementation with vitamin C on intestinal anastomosis healing in malnourished rats. METHODS: Male Wistar rats were divided into three groups: (1) sham, well-nourished rats that received vehicle; (2) FR+Veh, rats that were subjected to food restriction and received vehicle; and (3) FR+VC, rats that were subjected to food restriction and received vitamin C. Four days before surgery, the animals received vitamin C (100 mg/kg/day) via gavage and underwent colon resection with anastomosis in a single plane. The survival rate of rats was monitored until day 7 after surgery. Regarding anastomosis tissues, we examined intra-abdominal adhesion index, hydroxyproline content, collagen density, inflammatory parameters, and oxidative damage to proteins and lipids. RESULTS: Malnutrition decreases body weight and increases mortality; the survival rate was 90 % in group 1, 60 % in group 2, and 80 % in group 3. Vitamin C was able to increase hydroxyproline concentration and density of collagen and decrease the intra-abdominal adhesion index, as well as the infiltration of neutrophils and oxidative damage to proteins in malnourished rats compared to group treated with vehicle. CONCLUSIONS: Preoperative vitamin C supplementation can improve the intestinal anastomosis healing, biochemical alterations, and prolong survival in rats subjected to food restriction.


Asunto(s)
Ácido Ascórbico/uso terapéutico , Colon/cirugía , Suplementos Dietéticos , Desnutrición/tratamiento farmacológico , Cuidados Preoperatorios , Recto/cirugía , Cicatrización de Heridas/efectos de los fármacos , Anastomosis Quirúrgica , Animales , Ácido Ascórbico/administración & dosificación , Ácido Ascórbico/farmacología , Peso Corporal/efectos de los fármacos , Colágeno/metabolismo , Colon/efectos de los fármacos , Colon/patología , Hidroxiprolina/metabolismo , Masculino , Desnutrición/complicaciones , Nitratos/metabolismo , Nitritos/metabolismo , Estrés Oxidativo/efectos de los fármacos , Peroxidasa/metabolismo , Ratas Wistar , Recto/efectos de los fármacos , Recto/patología , Adherencias Tisulares/complicaciones , Adherencias Tisulares/tratamiento farmacológico , Factor de Necrosis Tumoral alfa/metabolismo
2.
Pathol Res Pract ; 212(9): 755-60, 2016 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-27475409

RESUMEN

OBJETIVE: The aim of this study was to evaluate the effects of diphenyl diselenide (PhSe)2 and ebselen (EB) in ulcerative colitis (UC) induced by dextran sulfate sodium (DSS) in rats. METHODS: The effects of (PhSe)2 and EB in rats submitted to DSS-induced colitis were determined by measurement of oxidative stress parameters, inflammatory response and bowel histopathological alterations. RESULTS: Animals developed moderate to severe neutrophil infiltration in histopathology assay in DSS rats and (PhSe)2 improved this response. Moreover, the treatment with (PhSe)2 decreased the oxidative damage in lipids and proteins, as well as reversed the superoxide dismutase (SOD) and catalase (CAT) levels in rats treated with DSS. EB was able only to reverse damage in lipids and the low levels of SOD in this animal model. CONCLUSIONS: The organoselenium compounds tested demonstrated an anti-inflammatory and antioxidant activity reducing the colon damage, being (PhSe)2 more effective than EB.


Asunto(s)
Azoles/uso terapéutico , Derivados del Benceno/uso terapéutico , Colitis/tratamiento farmacológico , Inflamación/tratamiento farmacológico , Compuestos de Organoselenio/uso terapéutico , Estrés Oxidativo/efectos de los fármacos , Animales , Azoles/farmacología , Derivados del Benceno/farmacología , Catalasa/metabolismo , Colitis/inducido químicamente , Colitis/metabolismo , Colon/efectos de los fármacos , Colon/metabolismo , Modelos Animales de Enfermedad , Inflamación/inducido químicamente , Inflamación/metabolismo , Isoindoles , Masculino , Neutrófilos , Compuestos de Organoselenio/farmacología , Ratas , Ratas Wistar , Especies Reactivas de Oxígeno/metabolismo , Superóxido Dismutasa/metabolismo
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